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A Pivotal Open-Label Trial of Brentuximab Vedotin for Hodgkin Lymphoma

Phase 2
Completed
Conditions
Disease, Hodgkin
Interventions
Registration Number
NCT00848926
Lead Sponsor
Seagen Inc.
Brief Summary

This is a single-arm, open-label, multicenter, pivotal clinical trial to evaluate the efficacy and safety of brentuximab vedotin (SGN-35) as a single agent in patients with relapsed or refractory Hodgkin lymphoma.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
102
Inclusion Criteria
  • Patients with relapsed or refractory Hodgkin lymphoma who have previously received autologous stem cell transplant.
  • Histologically confirmed CD30-positive disease; tissue from the most recent post diagnostic biopsy of relapsed/refractory disease must be available for confirmation of CD30 expression via slides or tumor block.
  • Fluorodeoxyglucose-avid disease by positron emission tomography and measurable disease of at least 1.5 cm as documented by spiral computed tomography.
  • At US sites patients greater than or equal to 12 years of age may be enrolled. At non-US sites patients must be greater than or equal to 18 years of age.
Exclusion Criteria
  • Previous treatment with brentuximab vedotin.
  • Previously received an allogeneic transplant.
  • Congestive heart failure, Class III or IV, by the New York Heart Association criteria.
  • History of another primary malignancy that has not been in remission for at least 3 years.
  • Known cerebral/meningeal disease.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Brentuximab vedotinbrentuximab vedotin-
Primary Outcome Measures
NameTimeMethod
Objective Response Rate by Independent Review Groupup to 12 months

Percentage of participants who achieved a best response of complete remission (CR, disappearance of all evidence of disease) or partial remission (PR, regression of greater than or equal to 50% of measurable disease and no new sites) per Cheson 2007 Revised Response Criteria for Malignant Lymphoma.

Secondary Outcome Measures
NameTimeMethod
Duration of Objective Response by Kaplan-Meier Analysisup to approximately 4 years

Duration of objective response (CR + PR) by independent review group, defined as time of initial response until disease progression or death.

Duration of Objective Response in Participants With Complete Remission by Kaplan-Meier Analysisup to approximately 4 years

Duration of response from start of first objective tumor response (CR or PR) by independent review group to disease progression or death due to any cause in participants with CR.

Overall Survivalup to approximately 6 years

Time from start of study treatment to date of death due to any cause.

Progression-free Survival by Kaplan-Meier Analysisup to approximately 4 years

Time from start of study treatment to disease progression per independent review group or death due to any cause.

Hematology Laboratory Abnormalities >/= Grade 3up to 12 months

Counts of study participants with post-baseline hematology laboratory abnormalities of Grade 3 or greater per NCI CTCAE version 3.0. Participants with multiple occurrences of a laboratory abnormality within a category are counted once in that category.

Time of Maximum Serum Concentration3 weeks

Time of maximum serum concentration from 0 to 21 days following the first dose of brentuximab vedotin

Complete Remission Rate by Independent Review Groupup to 12 months

Percentage of participants who achieved a best response of CR (disappearance of all evidence of disease) per Cheson 2007 Revised Response Criteria for Malignant Lymphoma.

Adverse Events by Severity, Seriousness, and Relationship to Treatmentup to 12 months

Counts of participants who had adverse events or treatment-emergent adverse events (TEAE, defined as newly occurring or worsening after first dose). Serious adverse events are reported from the time of informed consent. National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE version 3.0) were used to assess severity (1=mild, 2=moderate, 3=severe, 4=life threatening/disabling, 5=death). Relatedness to study drug was assessed by the investigator (Yes/No). Participants with multiple occurrences of an adverse event within a category are counted once within the category.

Chemistry Laboratory Abnormalities >/= Grade 3up to 12 months

Counts of study participants with post-baseline chemistry laboratory abnormalities of Grade 3 or greater per NCI CTCAE version 3.0. Participants with multiple occurrences of a laboratory abnormality within a category are counted once in that category.

Area Under the Curve3 weeks

Area under the serum concentration-time curve from time 0 to 21 days following the first dose of brentuximab vedotin

Maximum Serum Concentration3 weeks

Maximum serum concentration from 0 to 21 days following the first dose of brentuximab vedotin

Trial Locations

Locations (27)

City of Hope National Medical Center

🇺🇸

Duarte, California, United States

Washington University School of Medicine

🇺🇸

St. Louis, Missouri, United States

Institut Paoli Calmettes

🇫🇷

Marseille, France

Stanford University Medical Center

🇺🇸

Palo Alto, California, United States

University of Rochester Medical Center

🇺🇸

Rochester, New York, United States

Loyola University Medical Center Cardinal Bernardin Cancer Center

🇺🇸

Maywood, Illinois, United States

Baylor Sammons Cancer Center

🇺🇸

Dallas, Texas, United States

Weill Cornell Medical College

🇺🇸

New York, New York, United States

Hospital Saint Louis

🇫🇷

Paris, France

Memorial Sloan Kettering Cancer Center

🇺🇸

New York, New York, United States

Centre Henri Becquerel

🇫🇷

Rouen, France

University of Texas MD Anderson Cancer Center

🇺🇸

Houston, Texas, United States

University of Miami

🇺🇸

Miami, Florida, United States

University of California at Los Angeles

🇺🇸

Los Angeles, California, United States

Ohio State University

🇺🇸

Columbus, Ohio, United States

University of Washington

🇺🇸

Seattle, Washington, United States

Princess Margaret Hospital

🇨🇦

Toronto, Ontario, Canada

UZ Gasthuisberg

🇧🇪

Leuven, Belgium

Cliniques Universitaires UCL de Mont-Goddine

🇧🇪

Yvoir, Belgium

B.C Cancer Agency

🇨🇦

Vancouver, British Columbia, Canada

Instituto di Ematologia ed Oncologia Medica

🇮🇹

Bologna, Italy

Mayo Clinic Rochester

🇺🇸

Rochester, Minnesota, United States

Oregon Health & Science University

🇺🇸

Portland, Oregon, United States

Rocky Mountain Cancer Center

🇺🇸

Denver, Colorado, United States

University of Alabama at Birmingham

🇺🇸

Birmingham, Alabama, United States

Karmanos Cancer Institute

🇺🇸

Detroit, Michigan, United States

Georgetown University

🇺🇸

Washington, District of Columbia, United States

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